Commercial Tech Transfers in OSD Manufacturing

Are you ready to unlock the secret to seamless commercial tech transfers in oral solid dosage manufacturing? In this webinar, industry experts will describe proven strategies for accelerated process validation, ensuring quality consistency, and making use of cutting-edge equipment. Whether you’re navigating regulatory hurdles or optimizing processes, this session will give you insights into the art of a successful pharmaceutical tech transfer.

Register Free: https://www.pharmtech.com/pt_w/commercial-tech-transfers

Event Overview:

This presentation will explore the critical aspects of manufacturing commercial tech transfers for the manufacture of oral solid dosage (OSD) products. It will provide insights into the progression of process validation for existing commercial products, ensuring consistent quality, and navigating regulatory requirements. The discussion will also highlight Lonza’s advanced equipment capabilities, showcasing the company’s role in streamlining tech transfers and enhancing operational efficiency.


Key Learning Objectives:

• Gain insight into the tech transfer process
• Learn about Lonza’s equipment capabilities
• Discover how to effectively navigate operational challenges

Who Should Attend:

• Regulatory affairs specialists
• Project managers
• Research and development teams
• Manufacturing engineers
• Validation engineers
• Principal scientists
• CMC leads

Speakers

Rebecca Peek
Manufacturing Science and Technology Senior Engineer
Lonza

Rebecca Peek is a seasoned engineering professional with more than a decade of industry experience in oral solid dosage (OSD) manufacturing and pharmaceutical operations. She brings a wealth of expertise in leading successful technology transfer projects, process validations, and driving commercial approvals. Rebecca has a strong foundation in biomedical engineering and managing complex initiatives that bridge technical and regulatory requirements. She is experienced in the intricacies of scaling up OSD production, optimizing manufacturing processes, and utilizing cutting-edge technologies to enhance operational efficiency. Rebecca is very experienced in the execution of end-to-end process validations, ensuring alignment with rigorous quality standards and regulatory compliance, directly contributing to the approval and launch of multiple OSD products. She routinely works with diverse cross-functional teams, including R&D, manufacturing, and regulatory affairs, to streamline workflows and processes. She holds a project management professional (PMP) certification.

Laura Treche
Manufacturing Science and Technology Engineer
Lonza

Laura Treche is a manufacturing science and technology engineer with a strong background in oral solid dosage manufacturing. With hands-on experience in technology transfer, process scale-up, and optimization, Laura has successfully supported the transition of products into commercial manufacturing, ensuring compliance with Good Manufacturing Practices (GMP) and regulatory standards. She is adept at troubleshooting, process validation, and continuous improvement, maintaining a strong commitment to product quality and operational efficiency. Laura works closely with cross-functional teams, including R&D, quality, and regulatory departments, to drive the successful commercialization of small molecules. She is an asset in aligning manufacturing processes with business goals and regulatory requirements.

Register Free: https://www.pharmtech.com/pt_w/commercial-tech-transfers